№ lp_2_1_13463
PEHO syndrome is a clinically and genetically diverse entity, representing a phenotypic end-point of various severe genetic encephalopathies, highlighting significant heterogeneity in clinical and genetic presentations.
Year: 2021
Region / city: Cambridge, United Kingdom
Theme: Genetics, Epilepsy, Neurology
Document Type: Research Article
Institution: Addenbrookes Hospital, University of Cambridge, North West Thames Regional Genetics Service, Royal Hospital for Children & University of Glasgow, Nottingham University Hospitals NHS Trust
Author: Manali Chitre, Michael S Nahorski, Kaitlin Stouffer, Bryony Dunning-Davies, Hamish Houston, Emma L Wakeling, Angela F Brady, Sameer M Zuberi, Mohnish Suri, Alasdair PJ Parker, C. Geoffrey Woods
Target Audience: Researchers, clinicians, medical professionals
Period of Validity: N/A
Approval Date: N/A
Modification Date: N/A
Price: 8 / 10 USD
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